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Department of Nuclear Medicine and Diagnostic Imaging, Graduate School of Medicine, Kyoto University, Kyoto; Biomedical Imaging Research Center, Fukui Medical University, Fukui; National Institute for Physiological Sciences, Okazaki; Tokyo Metropolitan Institute of Gerontology, Tokyo; Hyogo Institute for Aging Brain and Cognitive Disorders, Hyogo; Aoba Brain Imaging Research Center, Telecommunications Advancement Organization, Sendai; Department of Nuclear Medicine and Radiology, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Japan
The aims of this study were to determine whether body weight or body surface area (BSA) should be used for noninvasive measurement of the cerebral metabolic rate of glucose (CMRGlc) by FDG PET with a standardized input function (SIF) and an autoradiographic method and to validate the procedure in a large population from different PET centers. Methods: Plasma input functions measured by intermittent arterial blood sampling after intravenous injection of FDG, in 101 patients from 1 institution who were fasting for at least 4 h, were used to generate the SIF. The SIF was generated by averaging over 101 patients the input function normalized with the net injected dose and initial distribution volume (DV) of FDG estimated by the formula c x Ha x Wb, where H is body height and W is body weight. To evaluate the estimation of DV by BSA or body weight, the coefficient of variation (CV) of the ratio of Ha x Wb to the measured DV was calculated by changing a and b independently. Estimation of the CMRGlc with SIF based on the formula for DV was validated with an additional 192 subjects from 3 institutions who underwent FDG PET while fasting. The result of simulation was compared with the results of 4 previously published formulas for BSA and body weight. Results: The optimal set of parameters, in which a was 0.80 and b was 0.35, minimized the CV. The averaged percentage error of the CMRGlc based on the optimal set of parameters for DV estimation and SIF was 8.9% for gray matter and 10.6% for white matter. Four BSA formulas brought about a similar error, which was significantly smaller than that based on body weight (P < 0.001, ANOVA). Conclusion: Noninvasive estimation of CMRGlc is made possible by careful measurement of the net injected dose and BSA.
Key Words: FDG PET initial distribution volume standardized input function glucose metabolism brain
Received Aug. 2, 1999; revision accepted Mar. 2, 2000.
For correspondence or reprints contact: Norihiro Sadato, MD, PhD, Biomedical Imaging Research Center, Fukui Medical University, Fukui, 910-1193, Japan.
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